Composition comprising salt of acyl glutamate as primary surfactant or primary anionic surfactant and specific structurant polymers

ABSTRACT

The present invention relates to compositions comprising salt of acyl glutamate as primary surfactant or primary anionic surfactant and specific structurant polymers.

FIELD OF THE INVENTION

The invention relates to personal care compositions. The compositions are preferably aqueous-based, isotropic, personal care compositions. The compositions are preferably mild (defined for example by low percent zein dissolved relative to harsher compositions). Preferably, the compositions have good foam volume (a signal of cleansing to many consumers), have good structure (defined by initial bulk viscosity) and are stable (defined by viscosity and clarity maintenance and no phase separation). Preferably, the compositions are clear at a pH of 6.5 and lower, preferably of 6.0 and lower (generally the pH of the composition may be from about 3 to 6.5). Preferably the pH is from about 3.5 to 6.0, more preferably from about 3.5 to 5.5, more preferably 4.0 to 5.5. In particular, the invention relates to use of specific structuring polymers required to ensure that low pH, clear (isotropic) compositions have good structure and stability, as noted, and remain clear.

BACKGROUND OF THE INVENTION

Synthetic detergents, such as cationic, anionic, amphoteric, non-ionic surfactants, are widely used in personal care cleaning compositions. Anionic surfactants generally exhibit superior cleansing and foaming properties and are thus typically incorporated into such compositions. Anionic surfactants, however, also tend to be harsh on the skin.

Since consumers desire milder compositions (i.e., compositions which are not as harsh and irritating on skin and skin proteins), it is known to replace some anionic surfactant with other surfactants (e.g., nonionic and/or amphoteric surfactants). Another approach is to associate anionic surfactants with amphoteric or cationic compounds to create surfactant complexes (see U.S. Pat. No. 4,443,362). Often these compositions suffer in foaming and/or cleansing performance.

Another approach for providing mildness is to use milder anionic surfactants. Among such mild anionic surfactants that can be used are N-acylamino acids and their salts.

The paper “Surface Active N-Acylglutamate: Preparation of Long Chain N-Acylglutamic Acid” (M. Takehaka et al.; Journal of the American Oil Chemists Society, Vol. 49, p. 157 ff) cites JP Patent No. 29444 (1964) according to which acyl glutamates are said to alleviate skin irritations caused by other anionic surfactants such as alkylbenzene sulfonates.

As seen in U.S. Pat. No. 6,703,427 to Schmucker et al., such acylamino acids are contemplated as co-surfactants to alleviate harshness of primary anionic surfactants. By themselves, as the primary surfactant (a “primary surfactant” is one which is present at a level of 50% or more of all surfactant) in a surfactant cleansing system (as is preferred for compositions of the invention), or as the primary anionic surfactant (as a “primary anionic surfactant”, the surfactant is present at 50% of all anionic surfactants; however, surfactants other than anionic surfactants may in total comprise greater than 50% of the entire surfactant system or less than 50% of the system), such surfactant would be expected to be deficient in foam and/or cleansing relative to use of other anionic surfactants in the same composition. Further, acylamino acids are difficult to solubilize at lower pH ranges because the molecule will tend to precipitate. It would generally not be contemplated thus to use acylamino acids such as glutamate at a low pH and, typically, salt of glutamate does precipitate at about a pH of 5.5 and lower. As such, such glutamate salt molecules would not be contemplated for use in isotropic liquids (where solubility is required to ensure good clarity) at any significant level. In particular, they would not be contemplated for use as primary surfactant, or as a primary anionic surfactant and where, simultaneously, the amount of glutamate is equal to or greater than, preferably greater than, any other single surfactant present. That is, according to our invention, if the salt of glutamate is primary anionic surfactant but the total sum of non-anionic surfactants is greater than that of anionic surfactant, the salt of glutamate must be present in an amount equal to or greater than any other surfactant present. It is preferred that the glutamate salt be present as the primary surfactant.

It would further not be contemplated to use acyl glutamate (unless specified otherwise, we use term “glutamate” or “acyl glutamate” to mean the salt of the glutamate) as a primary surfactant or as a primary anionic surfactant (where glutamate is simultaneously present in an amount equal to or greater than any other single surfactant present), because glutamate does not structure (e.g., self-structure) as readily as other surfactants and therefore can make it more difficult to suspend particles and other benefit agents. Further, it is not readily apparent how to structure with external structurants while maintaining a relatively clear, isotropic liquid, particularly at a low pH (e.g., of 6.5 and lower, preferably 6.0 and lower). The subject application relates to compositions where glutamate is the primary surfactant (and by definition the primary anionic surfactant) and in which specific structuring polymers are used to provide good structuring (defined by initial bulk viscosity) and stability (defined by viscosity and clarity maintenance and no phase separation) of the liquids while maintaining desired clarity (at low pH of 6.5 and lower, preferably of 6.0 and lower, more preferably of 4.0 to 5.1).

In short, because acyl glutamate surfactants are not the type of anionic surfactants which provide superior foaming, because they do not readily solubilize (at lower pH), and because they do not self-structure as well as other anionics, such surfactants would not have been considered for use in a low pH (pH of 6.5 and lower) liquid cleansing composition as the primary surfactant; or as primary anionic surfactant, but where the amount of glutamate is present in amounts equal to or greater than any other single surfactant present. In particular, they would not be contemplated for use as primary or primary anionic surfactant in aqueous-based cleansing compositions while retaining the ability to maintain good structure, stability and clarity.

Unexpectedly, applicants have found that it is possible to formulate low pH, aqueous-based isotropic compositions (which are structured, stable and clear) in which acyl glutamate is primary surfactant (preferred systems); or primary anionic surfactant and simultaneously present in an amount equal to or greater than any other single surfactant present. According to the subject invention specific structuring polymers are used. Preferably, the pH of the composition is 6.5 and lower. More preferably, of pH is 3.5 to 6.0. More preferably, pH is 3.5 to 5.5 and most preferably 4.0 to 5.5, even more preferably 4.0 to 5.1. Preferably, the composition is visibly clear (isotropic). Preferably, the composition is a single phase (single phase which is isotropic), clear composition where clarity is defined by an absorbance value of 1.0 or lower, preferably 0.5 or lower (e.g., 0.01-0.5), more preferably 0.2 and below when measured at wavelength of 550 nm. Use of specific structuring polymers permits clarity to be maintained while maintaining good structure (i.e., initial bulk viscosity) and stability (i.e., viscosity and clarity maintenance under defined conditions and no phase separation under defined conditions).

Further, applicants have found that, when the amount of shorter chain glutamate (as a percent of all glutamate) is minimized (to ensure good foam) and the percent of glutamate relative to co-surfactant is maximized (saving on cost of use of co-surfactant while surprisingly maintaining low pH, clear, one phase isotropic compositions), preferred compositions are found. In preferred systems, glutamate is the primary surfactant (present at level of 50% or more, preferably 55% or more of all surfactant). Preferred systems comprising glutamate and particular co-surfactants are also disclosed.

In the subject application, applicants disclose compositions in which specific polymers can be used to ensure structured, stable, isotropic liquids which are formed at relatively low pH (of pH 6.5 and lower, preferably pH of 6.0 and lower, preferably pH of 5.5 and lower) while also maintaining defined level of clarity. As noted, these compositions are stable as defined in at least two ways. They are stably structured in that, using structurants of the invention, they have initial bulk viscosity of at least 1000 cps, and they are stable in that compositions maintain viscosity and clarity and do not separate under defined conditions. Such structured, stable and clear compositions would not be expected to form in systems where glutamate is the primary surfactant, or the primary anionic surfactant while simultaneously present in an amount equal to or greater than any other single surfactant present.

As noted, stability is defined in part to include maintenance of clarity. Thus, when we define compositions as structured, stable and clear, this is simply to emphasize the importance of both clarity initially and over time.

A variety of compositions have been disclosed where glutamate is disclosed broadly.

In U.S. Pat. No. 6,284,230 to Sako et al. a broad number of surfactants, including glutamates are said broadly to be able to be used as primary anionic surfactant. From the examples however, it is clear that where glutamate is used (Examples I-V), it is neither the primary surfactant (ammonium sulfate is in Examples I-V) nor is it the primary anionic surfactant. In Example VI, sarcosinate (different acyl amino acid with a single carboxylic acid group) is the primary surfactant. Never is an acyl amino acid having two carboxylic acid groups (such as glutamate) used as primary surfactant or as primary anionic surfactant in which the glutamate is used in an amount equal to or greater than any other single surfactant present.

US 2004/0258807 and US 2011/016506 are two other examples of references disclosing glutamates broadly but again it is clear that glutamates are never used as primary surfactants; or as primary anionic surfactant and where glutamate is simultaneously present in an amount equal to or greater than any other single surfactant present in the composition.

US 2005/034895 shampoo compositions comprise surfactant, microbiological control agent, rheological additive, conditioning agent and solubilizer. The surfactant compositions include mixtures of glutamate and other surfactants (see Examples 2-5), but glutamate is never primary surfactant or primary anionic where it is used in amounts equal to or greater than any other single surfactant in the composition.

WO 2010/069500 discloses in Example 1, Composition E, a composition having 3.5% glutamate, 3.5% sarcosinate, 8.5% betaine and 2.5% glucoside. In this composition glutamate is primary anionic (is present at level of 50% of anionic), but is not present in an amount equal to or greater than any other single surfactant present (e.g., betaine is single greatest surfactant present). It is also not the primary surfactant.

The present invention, as noted, requires the glutamate be either primary surfactant (preferred embodiment); or present as primary anionic surfactant while simultaneously being used in an amount equal to or greater than, preferably greater than, any other single surfactant present in the composition. For reasons noted above, formation of such system would not be contemplated because such systems where glutamate is used (especially as primary surfactant) in such relatively large amounts would have been thought to compromise the formation of compositions which are clear (isotropic), foam well, are well structured (i.e., defined by initial bulk viscosity) and are stable (defined by both viscosity and clarity maintenance as well as by absence of visible phase separation). Further it was unexpected that specific structuring polymers work so well to ensure structure and stability of the composition while also maintaining low pH, clear, isotropic composition (clarity maintenance as noted being encompassed by definition of stability).

SUMMARY OF THE INVENTION

The present invention relates to personal care cleansing compositions comprising:

-   -   1) 0.5-35% of a surfactant system wherein the anionic surfactant         is present at 0.5 to 25%, preferably 1 to 15% by wt. of the         total composition and where         -   a) the salt of acyl glutamate is present at 50% or greater             of all the surfactant present (“primary surfactant”); or         -   b) is present at level of 50% or more of the anionic             surfactant (preferably the salt of acyl glutamate comprises             greater than 50% by wt. of the anionic, more preferably             greater than 60% by wt. of total anionic) and simultaneously             is present in an amount equal to or greater than any other             single surfactant present in the composition (“primary             anionic surfactant”);     -   2) 0% to 20%, preferably 0.5 to 15% by wt. of a co-surfactant         selected from the group consisting of nonionic, cationic and         amphoteric surfactant and mixtures thereof (preferably, the         co-surfactants comprise amphoteric surfactant, optionally         further comprising nonionic; preferably amphoteric comprises         1-10% by wt. of total composition);     -   3) optionally, 0 to 30%, preferably 0.1-10%, more preferably         0.1-5% of a skin or hair benefit agent;     -   4) 0.1 to 10% of a structuring polymer which is a polymerization         product of:         -   a) 0 to 10% by wt. of total monomer of a first ethylenically             unsaturated monomer selected from the group consisting of:             -   i. diacids of formula HOOC—CR¹═CR²—COOH (I);             -   ii. a cyclic anhydride precursor of diacid (I), having                 the formula:

-   -   -   -   iii. and combination thereof, where

        -   R¹ and R² are individually selected from H, C₁-C₃ alkyl,             phenyl, chlorine and bromine;

        -   b) 15 to 60% by wt. of total monomer of a second             ethylenically unsaturated monomer selected from the group             consisting of acrylic acid, methacrylic acid and mixtures             thereof;

        -   c) 30 to 75% by wt. of total monomer of a (meth)acrylate             monomer which is selected from the group consisting of C₁ to             C₈ esters of acrylic acid, C₁ to C₈ esters of methacrylic             acid and mixtures thereof; and

        -   d) 1 to 25% by wt. of total monomer of an associative             monomer having the formula:             R⁴—CH═C(R³)—C(O)—O—(R⁵O)_(a)—R⁶             -   wherein:                 -   R³ and R⁴ are independently selected from H and C₁₋₃                     alkyl,                 -   each R⁵O is independently an oxyalkylene unit having                     from 2 to 4, preferably from 2 to 3 carbon atoms,                 -   R⁶ is selected from:                 -    linear and branched alkyl having from 8 to 40,                     preferably from 8 to 30, more preferably from 10 to                     22 carbon atoms, and                 -   alkaryl, the alkyl group of which has from 8 to 40,                     preferably from 8 to 30, more preferably from 10 to                     22 carbon atoms, such alkyl group being linear or                     branched, said alkaryl preferably being alkylphenyl;                     and                 -   a has a value of from 6 to 40, preferably from 15 to                     35, most preferably from 20 to 30.

    -   5) balance water         -   wherein pH is 6.5 and lower, preferably wherein pH is 6.0             and lower, more preferably, wherein pH is 5.5 and lower,             more preferably where pH is 5.1 and lower.         -   A preferred pH range is about 3.5 to 5.5, preferably 4.0 to             5.5, especially 4.0 to 5.1.

When specific co-surfactants are used, certain levels of fatty acid and/or salts may also be required.

With regard to use of optional oil or emollient of component (3), applicants first note that the invention may be defined as a surfactant chassis which itself is based on acyl glutamate as primary surfactant or primary anionic surfactant. The surfactant chassis is preferably a stable, single phase, optically clear (isotropic) composition. However, when certain optional components (e.g., certain oils or emollients) are added to the surfactant chassis, these may not be completely miscible with the stable, isotropic, surfactant chassis and may render the resulting full formulation anisotropic (e.g., the composition is no longer “clear”).

Thus, the invention may comprise a full formulation which contains no oil or emollient; or which contains a sufficiently low amount of oil or emollient; or which contains an oil or emollient which is miscible with the surfactant chassis so as not to become anisotropic as noted above. This formulation is a stable, single phase composition which is clear (isotropic) as defined by an absorbance value of 1.0 or lower at defined wavelength.

The compositions of the invention could preferably comprise immiscible benefit agent. The invention also comprises a full formulation which is anisotropic (not optically clear) but which is formed from the combination of (1) a stable, single phase, surfactant chassis, which is preferably optically clear; and (2) optional ingredient(s) present in sufficient amount to render the final full formulation anisotropic. A final anisotropic formulation which is not formed from the structured, stable, single phase, optically clear surfactant chassis is not considered part of the subject invention. Specifically, a composition which is anisotropic before addition of, for example, emollient or oil is not part of the invention.

Preferably, compositions of the invention (whether isotropic at full formulation or isotropic at chassis formation and anisotropic upon addition of certain benefit agents) are, or are formed from single phase isotropic systems. Preferably, the compositions (again, as final composition, or as isotropic chassis before addition of potential anisotropic forming benefits agents) maintain optical clarity. Preferably the compositions (as final isotropic composition or isotropic chassis) are single phase systems which maintain optical clarity as defined herein. Preferably, structure, stability and clarity are maintained in the presence of specifically claimed structuring polymers of the invention. Preferably the single phase, optically clear systems have initial bulk viscosity defining good structuring, maintain viscosity and clarity (±30% of initial values) when measured at various temperatures after two weeks, and remain visibly homogeneous when measured at various temperatures after two weeks.

In typical preferred compositions of the invention, the amount of glutamate surfactant is equal or is in excess of all other surfactants (“primary surfactant”); it may also be present at 50% or more of anionic and simultaneously present in amount equal to or greater than any one other single surfactant (“primary anionic surfactant”). Even if the sum of surfactants other than anionic form more than 50% of the surfactant system, glutamate must be present in an amount equal to or greater than any other single surfactant. It is preferred, however, that glutamate be the primary surfactant. It is preferred to maximize the amount of glutamate used and minimize use of cosurfactants.

Compositions of the invention contain 0.1 to 10% of the specific structuring polymers noted above. Compositions comprising the specific structurants surprisingly maintain clear, isotropic liquids which are both phase stable and are stably structured (as defined by viscosity and viscosity maintenance), all at defined low pH range.

Compositions of the invention may additionally comprise 0 to 10% by wt., preferably 0.1 to 10% by wt., more preferably 0.5 to 7% by wt. of structurant. Such structurant may be water soluble or water dispersible polymer which can be a cationic, anionic, amphoteric or nonionic polymer for enhancing viscosity and stability of the cleanser and is selected from the group consisting of carbohydrate gums; modified and non-modified starch granules; polyacrylate and methacrylate polymer and copolymer; cationic polymers including cationic modified polysaccharide, cationic modified cellulose and synthetic cationic polymers. These additional structurants need not be present although it is preferred for stabilizing the composition and helping to suspend, especially to suspend oil soluble emollients.

Compositions of the invention may comprise water-soluble skin or hair benefit agents. These may be present at levels of 0-30%, preferably 0.1-20% by wt., more preferably 0.1 to 10% by wt. total composition. Some compositions comprise water-soluble polyhydroxy alcohols. Preferred water soluble skin benefit agents include glycerin, sorbitol and polyalkylene glycols (a preferred polyalkylene glycol is polyethylene glycol) and mixtures thereof. Preferably, oil soluble emollients comprise 30% or less, preferably 10% or less, preferably 5% or less (e.g., 0.1 to 5% by wt.) of composition. In some preferred embodiments, oil soluble emollients or oils are absent.

In the absence of immiscible benefit agents (such as oil soluble emollient or oils), the final compositions are clear (isotropic). They may remain so if the quantities of immiscible ingredients are sufficiently small. However, even though the surfactant chassis is clear, the invention also contemplates full formulations which may be anisotropic but are formed from the combination of isotropic surfactant chassis and sufficient amounts of immiscible benefit agent to render the full formulation anisotropic.

DETAILED DESCRIPTION OF THE INVENTION

The invention relates to low pH cleansing compositions, preferably aqueous-based and clear, wherein salts of acyl glutamate are present as “primary surfactant” or, where the glutamate salts are “primary anionic surfactants” (although non-anionic may be present at greater than all anionic surfactants) and are simultaneously present in an amount equal to or greater than any other single surfactant present. When glutamate is not present in an amount equal to greater than any other single surfactant, such composition is not intended to be encompassed by compositions of the invention.

More specifically, the compositions comprise specific structuring polymers which maintain clarity of the low pH isotropic compositions as well as structure (defined by initial bulk viscosity) and stability (defined by maintenance of viscosity and clarity when tested under defined conditions and maintenance of homogeneity and integrity without visible phase separation). Preferably (especially when using particular co-surfactants, e.g., betaine versus amphoacetate), minimum amounts of free fatty acids are used to ensure structure, clarity, and stability.

Whether or not the glutamate is primary surfactant, or primary anionic surfactant while simultaneously present in amounts equal to or greater than any other single surfactant, it is seen that glutamate necessarily comprises 50% or greater of all anionic surfactant present and, as noted, is present in an amount equal to or greater than, preferably greater than, any other single surfactant in the composition. Because of the properties of glutamate noted above, it would not have been previously contemplated to form low pH compositions where glutamate is primary surfactant or primary anionic surfactant while maintaining structured, stable, single phase, clear (isotropic) formulations. In some preferred compositions, the amount of short chain glutamate (C₁₀ or below) is minimized (to enhance foaming). Particular structurants are used to enhance stability and structuring (while maintaining clarity), even at very low pH.

Although glutamate surfactants are milder than other anionic surfactants, they do not typically foam or cleanse as well. Like all acylamino surfactants, acyl glutamates are also difficult to solubilize at low pH and would therefore not be contemplated for use in low pH, clear (isotropic) compositions (i.e., lack of solubility would be believed to affect clarity), particularly at the relatively high levels of glutamate surfactant required in the subject invention. This is especially true where glutamate is the primary surfactant.

Unexpectedly, applicants have now produced low pH, structured, stable, clear (isotropic) compositions (as final formulation or as surfactant chassis prior to addition of anisotropic inducing agents) wherein glutamate is the primary surfactant or primary anionic surfactant and present in an amount equal to or greater than any other single surfactant. Preferred compositions maximize the amount of glutamate used (as percent of total surfactant) in order to minimize costly co-surfactant. Further, preferred compositions minimize the amount of shorter chain length glutamate used and thereby enhance foaming. In preferred compositions, using specific structurants allows use of maximum amounts of glutamate in clear, single-phase compositions (as final composition or as surfactant chassis) and particularly at low pH (e.g., of 5.5 and lower, preferably 5.0 and lower) all while maintaining clarity, structure (initial bulk viscosity) and stability (defined by maintenance of viscosity and clarity and by no visible phase separation). In some preferred systems, the amount of benefit agents, particularly oil or oil soluble emollient is minimized (0 to 30%, preferably 0 to 10%, preferably 0 to 5% by wt., preferably absent).

More specifically, compositions of the invention comprise:

-   -   1) 0.5 to 35% by wt. of total composition of a surfactant system         (surfactant chassis) wherein the anionic surfactant is present         at 0.5 to 25%, preferably 1 to 15% by wt. of total composition         and wherein salt of acyl glutamate         -   a) is present at 50% or more, preferably 60% or more, more             preferably 65% or more of all surfactant present (“primary             surfactant”); or is present at 50% or more, preferably             greater than 50%, more preferably greater than 60% of the             anionic surfactant and is simultaneously present in amount             equal to or greater than any other single (non-anionic)             surfactant in the composition (“primary anionic             surfactant”); for purposes of this definition, if the             glutamate and the second anionic surfactant both comprise             50%, glutamate is still considered a “primary anionic             surfactant”; and         -   b) 0% to 20%, preferably 0 to 15% by wt. of a co-surfactant             selected from the group consisting of nonionic, cationic and             amphoteric surfactants and mixtures thereof; preferably             there is present amphoteric surfactant as 1-10% by wt. of             total composition. By co-surfactant is meant surfactant             separate from the glutamate and separate from any additional             anionic surfactant which define component (a) above (i.e.,             although other anionic surfactants comprise part of             component (a) and are used in amount 50% or less of total             anionic, component (b) is concerned with surfactants which             are not anionic);             -   Depending on particular co-surfactants used (and to some                 extent the chain length of glutamate salts), the amount                 needed to optimize isotropic systems can vary. For                 example, as seen in the examples, in a system with                 glutamate and amphoacetate, the amount of amphoacetate                 to glutamate required to maximize isotropic region can                 be in ratio of 1/7 (e.g., 12.5% amphoacetate to 87.5                 glutamate; see Table 2) (using mix of decanoyl and                 cocoyl glutamate) and higher or even 1/1.7 (even more                 amphoacetate; using mix of decanoyl and lauroyl, see                 Table 1) and higher (up to 1/1); by contrast when using                 CAPHS or cocoyl betaine, much less co-surfactant can be                 used (e.g., ratio of 1/19 and higher, see Tables 4 and 5                 where stable regions are obtained at 5% CAPHS or                 cocoylbetaine and 95% glutamate) while maximizing                 isotropic region.             -   The above are non-limiting examples of some                 co-surfactants which may be used and, as noted, are not                 intended to limit the invention in any way.     -   2) optionally 0.0 to 30%, preferably 0.1 to 20%, more preferably         0.1 to 10% by wt. of a skin or hair benefit agent; preferably         the benefit agent is an oil-soluble emollient or moisturizing         oil (although water-soluble agents may also be used). Preferably         it is petrolatum or silicone. Also preferably, the oil is a         vegetable or triglyceride oil. Preferred oils include sunflower         seed oil and soybean oil. Other oils are noted below. Preferably         the emollient can be an ester of long chain (e.g., C₁₄-C₃₀)         fatty acid such as isopropyl palmitate or cetyl lactate;         combinations of any of the above are preferred;     -   3) 0.1 to 10% of a structuring polymer which is a polymerization         product of:         -   a) 0 to 10% by wt. total monomer of a first ethylenically             unsaturated monomer selected from the group consisting of:             -   i. diacids of formula HOOC—CR¹—CR²═COOH (I);             -   ii. a cyclic anhydride precursor of diacid (I), having                 the formula:

-   -   -   -   iii. and combination thereof, where             -   R¹ and R² are individually selected from H, C₁-C₃ alkyl,                 phenyl, chlorine and bromine;

        -   b) 15 to 60% by wt. total monomer of a second ethylenically             unsaturated monomer selected from the group consisting of             acrylic acid, methcyclic acid and mixtures thereof;

        -   c) 30 to 70% by wt. total monomer of a (meth)acrylate             monomer which is selected from the group consisting of C₁ to             C₈ esters of acrylic acid, C₁ to C₂ ester of methacrylic             acid and mixtures thereof; and

        -   d) 1 to 25% by wt. total monomer of an associative monomer             having the formula:             R⁴—CH═C(R³)—C(O)—O—(R⁵O)_(a)—R⁶             -   wherein:                 -   R³ and R⁴ are independently selected from H and C₁₋₃                     alkyl,                 -   each R⁵O is independently an oxyalkylene unit having                     from 2 to 4, preferably from 2 to 3 carbon atoms,                 -   R⁶ is selected from:                 -    linear and branched alkyl having from 8 to 40,                     preferably from 8 to 30, more preferably from 10 to                     22 carbon atoms, and                 -    alkaryl, the alkyl group of which has from 8 to 40,                     preferably from 8 to 30, more preferably from 10 to                     22 carbon atoms, such alkyl group being linear or                     branched, said alkaryl preferably being alkylphenyl;                     and             -   a has a value of from 6 to 40, preferably from 15 to 35,                 most preferably from 20 to 30; and

    -   4) balance water and other ingredients as defined below         -   wherein pH of composition is 63 and below, preferably 6.0             and below, more preferably 5.5 and below; preferably pH is             3.5 to 6.0, more preferably 3.5 to 5.5, more preferably 4.0             to 5.5.

As indicated, the amount of glutamate may be such that it is the primary surfactant; or glutamate may be the primary anionic surfactant, while the amount of surfactant other than anionic may be in excess of the glutamate. Where glutamate is the “primary anionic surfactant”, but the surfactant system has less than 50% anionic surfactant overall, glutamate must be present in amount equal to or greater than any other single surfactant present in the composition.

Further, the compositions of the invention are clear (isotropic) one-phase solutions. That is, there is one single clear phase (rather than one phase which is clear as part of a multi-phase solution). The phase is stable (maintains viscosity and clarity and does not break into multi-phases). Use of specific polymer ensures that compositions are clear, stably structured and maintain stability. By clear is meant having absorbance value of 1.5 or lower, preferably 1.0 or lower, more preferably 0.5 and below when measured at wavelength of 550 nm.

If benefit agent component (2) is not completely miscible in the surfactant chassis of (1), the composition may be anisotropic. However, the invention is defined either by presence of component (2) which is miscible so that final formulation is isotropic or by final anisotropic composition which was formed from combination of isotropic chassis of component (1) and benefit agent of component (2). The key to invention, however, is formation of final composition (isotropic; or anisotropic from an isotropic chassis defined by components (1), (3) and (4)) having a pH and clear, structured, stable one-phase isotropic characteristics defined.

When certain co-surfactants are used, it may be necessary to use minimum levels of fatty acid (e.g., lauric or myristic) or minimum levels of magnesium chloride. For example, when CAPB is co-surfactant, 0.1 to 2% by wt. fatty acid (C₁₀-C₁₄) may be used or 0.8-3% by wt. MgCl₂.

Surfactant System

Anionic Surfactant

A key to the invention is that there is present 0.5 to 35% by wt. of total composition of a surfactant system wherein anionic surfactant comprises 0.5 to 25% by wt. of total compositions and wherein salt of acyl glutamate comprises 50% or more of all surfactant (“primary surfactant”); or 50% or more, preferably 60% or more by wt. of the total anionic surfactant present (even if anionic overall is less than 50% of total surfactant) and is present in an amount equal to or greater than any other single surfactant in the composition. Preferably anionic surfactant comprises 1-15% by wt. of total composition, more preferably 2 to 12% of total composition. In some compositions, anionic comprises 5-12% by wt. of the total composition and surfactants which are not anionic comprise 1 to 7% by wt. of the composition. The amount of glutamate should always be maximized and, as noted, even if other surfactants are present in amounts greater than anionic (e.g., when glutamate is not the “primary surfactant”), glutamate is present at 50% or more of anionic surfactant and is present in an amount equal to or greater than any other single surfactant present.

The salt of acyl glutamate used in the composition of this invention has a structure as follows:

(It is noted that one or the other structures will occur at pH levels of the invention (pH 6.5 and below, preferably 3 to 6.5) and that at higher pH (e.g., 8 or 9), some di-salt is also present),

-   -   where R is alkyl or alkenyl group (generally saturated although         some unsaturated, for example, oleoyl, may be present) having 8         to 20 carbons, preferably 8 to 16 carbons, more preferably 10 to         14 carbons. Preferably, R is predominantly a mixture of C₁₀ to         C₁₄. As indicated above, for preferred levels of foaming, it is         preferable to minimize the amount of shorter chain length (e.g.,         C₈ and C₁₀) and to maximize longer chain length, e.g., C₁₂-C₂₀,         preferably C₁₂-C₁₅. Although C₁₀ should be minimized, it will be         seen, at least in some embodiments of the invention, that ratio         of C₁₀ to C₁₂ should be at least 1/5, possibly 1/3 and higher         (in part depending on co-surfactant used with glutamate salts)         to ensure isotropic formation. Preferably ratio should be no         higher than 1 to 1, regardless of co-surfactant used with         glutamate salts. As also used in the examples, a cocoyl chain         length distribution is typically defined here as follows: 13%         C₈-C₁₀, 50% C₁₂, 18% C₁₄, 8% C₁₆, and 11%≥C₁₈,         (http://coconutboard.nic.in/English-Article-Gopalakrishna-CFTRI.pdf),         as preferred here.

M is a solubilizing cation such as, for example, sodium, potassium, ammonium or substituted ammonium. It is preferred that the cation is sodium or potassium, more preferably sodium. Sodium salt is preferred.

The pH of the overall composition is typically 6.5 and lower, preferably 6.0 and lower. Preferably pH is 3 to 6.5 and more preferably 3 to 6. More preferably, pH is 3.5 to less than 6, preferably 3.5 to 5.5, more preferably 4.0 to 5.5, even more preferably 4.0 to 5.1.

The pKa of the salt of acyl glutamate is relatively low (about 5). Applicants have surprisingly found that the relatively large amounts of glutamate used can be solubilized thereby allowing to take advantage of the mildness of this anionic surfactant relative to other anionic surfactants.

Further, surprisingly large amounts of glutamate can be solubilized at low pH, thereby permitting formation of clear, one-phase isotropic compositions (which are structured and stable) which are also mild.

Clear and mild cleansers are seen as highly desirable by consumers. By clarity, applicants mean having absorbance value of 1.0 or lower, preferably 0.5 or lower, even more preferably 0.2 or lower when measured at wavelength of 550 nm. As indicated above, clarity values define the surfactant chassis and water. Composition may maintain clarity (stay isotropic) upon addition of benefit agent but, even if final composition is anisotropic, if the initial chassis was isotropic as defined, it falls within definition of the invention.

While the acyl glutamate salt may be used as the only anionic surfactant in the total composition, it is desirable to use other anionic surfactants, subject to the levels defined here.

One preferred co-anionic (as opposed to co-surfactant 1(b)) is sarcosinate (alkyl salt of C₁₀-C₁₄ acyl sarcosinate is a preferred sarcosinate, where salt is defined as in M above). Another preferred co-anionic is a taurate. A salt of C₁₀-C₁₄ acyl taurates (e.g., sodium cocoyl methyl taurates) is preferred. Generally, it is preferred not to use salts which would tend to precipitate at lower pH values. Thus, it is preferred to minimize, for example, the amount of acyl glycinate (<1.0%, preferably <0.5%, preferably absent altogether).

Generally, sarcosinate have formula: R²CON(CH₃)CH₂CO₂M;

Taurates have formula: R²CONR³CH₂CH₂SO₃M;

-   -   where R³ is methyl

Glycinates have formula: R²CONHCH₂CO₂M

-   -   where R² above is alkyl or alkenyl having 8 to 22 carbons,         preferably 12 to 18 carbons; and

M is solubilizing cation as defined above.

Compositions of the invention may have low levels of alkyl ether sulfates, for example, sodium lauryl ether sulfate. By low is meant <20% of anionic, preferably <10%, more preferably <5%. In some embodiments the compositions have <0.5% alkyl ether sulfate and in some there is substantially no alkyl ether sulfate. These type of sulfates are preferably minimized because they are less mild than other surfactants.

Co-Surfactant

A second component of the invention may comprise 0% to 20%, preferably 0.5 to 15% by wt. of total composition of a co-surfactant selected from the group consisting of non-ionic, cationic, and amphoteric surfactant and mixtures thereof.

Preferred co-surfactants are amphoteric or zwitterionic surfactant. Preferably the co-surfactant is amphoteric.

This general class of amphoteric detergents has the following general structure:

-   -   where R is an alkyl or alkenyl radical of 7 to 17 carbons or a         carboxamido functional group of the general structure

-   -   where R₁ is an alkyl or alkenyl radical of 7 to 17 carbons and         R₄ is an alkyl, hydroxyalkyl, or carboxyalkyl radical of 1 to 3         carbons. R₂ and R₃ are each independently a proton, an alkyl,         hydroxyalkyl, or carboxyalkyl radical of 1 to 3 carbons, or is         missing entirely, subject to the following restraints. When R₂         and R₃ are each independently an alkyl, hydroxyalkyl, or         carboxyalkyl radical, the nitrogen in a quaternary amine and is         a cationic charge center. When one of R₂ or R₃ is an alkyl,         hydroxyalkyl, or carboxyalkyl radical and the other is a proton         or is missing entirely, the nitrogen is a tertiary amine. At a         pH well below the pK_(a) of the tertiary amine, the other of R₂         or R₃ will be a proton and the amine will be a cationic charge         center. At a pH well above the pK_(a) of the tertiary amine, the         other of R₂ or R₃ will be missing entirely and the amine will be         a neutral charge center.

Preferred examples of amphoteric noted above include cocoamidopropylbetaine (CAPB), C₁₀-C₁₄ alkyl betaine, the salt of C₁₀-C₁₄ alkyl amphoacetate (e.g. lauroamphoacetate) and mixtures thereof.

When CAPB is used, there also should be used 0.1-2.0% by wt. fatty acid or 0.8-3% magnesium chloride to ensure the clear compositions of the invention are formed.

Another class of amphoteric detergents are the sultaines having the following general structure:

-   -   where R is an alkyl or alkenyl radical of 7 to 17 carbons or a         carboxamido functional group of the general structure

-   -   where R₁ is an alkyl or alkenyl radical of 7 to 17 carbons and         R₄ is an alkyl, hydroxyalkyl, or carboxyalkyl radical of 1 to 3         carbons. R₂ and R₃ are each independently an alkyl,         hydroxyalkyl, or carboxyalkyl radical of 1 to 3 carbons, so that         the nitrogen in a quaternary amine and is a cationic charge         center. A preferred amphoteric surfactant of this class is         cocamidopropyl hydroxy sultaine (CAPHS), lauramidopropyl hydroxy         sultaine (LAPHS), or lauryl hydroxy sultaine (LHS).

A preferred combination of the invention is salt of glutamate and salt of sarcosinate as anionic surfactants in combination with salt of amphoacetate (preferably C₁₀C₁₄ amphoacetate) as co-surfactant. A preferred combination comprises 3-8% by wt. total composition salt of glutamate, 1-3% by wt. total composition salt of sarcosinate (where, preferably, glutamate is the primary surfactant or primary anionic as defined above) and 3-8% by wt. total composition salt of amphoacetate (particularly alkali metal salt of acyl amphoacetate). As previously noted, glutamate is present in an amount equal to or greater than any other single surfactant present.

A key aspect of compositions of the invention is that (as full isotropic composition, or as surfactant chassis prior to forming composition) they are structured, stable, clear, one-phase isotropic liquids, particularly at pH values of 6.5 and lower, preferably pH of 3.5 to 6.0, more preferably 3.5 to 5.5, more preferably 4.0 to 5.5.

The glutamate salts may comprise a mixture of chain lengths. As indicated, it is typically preferably to minimize shorter C₈ and C₁₀ lengths as these do not typically foam as well. Using a mixture of C₁₀ and cocoyl also helps to extend regions of isotropic clarity compared to mixtures where only, for example, C₁₀ and C₁₂ are used. This suggests that some amount of C₁₄ to C₂₀ may also be preferred.

In some compositions, the surfactant system comprises a mixture of C₁₀ and cocoyl glutamate together with alkali metal salts of amphoacetate.

Primarily, the invention is about the unexpected observation that glutamate may be used as primary surfactant; or as primary anionic surfactant and is simultaneously used in an amount equal to or greater than any other single surfactant present in the composition. Preferably it is used as primary surfactant in low pH, aqueous-based single-phase, compositions having visual clarity. Even if added benefit agent causes formation of final anisotropic composition, the surfactant chassis, prior to addition of anisotropic forming agent, is isotropic. Because of their low pH solubility, it is thus possible to make a mild composition (acylamino surfactant being mild) which is also optically clear (isotropic). At the same time, because these are low pH compositions, they can provide antibacterial effect while avoiding use of certain antibacterial agents which are restricted in certain parts of the world. Further, the invention comprises use of specific structuring polymers to ensure clarity and viscosity are maintained while also maintaining no visible separation.

Thus, anisotropic compositions (formed using glutamate-based isotropic chassis) with low pH and low pH compatible preservation systems are another aspect of the invention.

Use of these milder glutamate surfactants at relatively high levels also permits that lesser amounts of cosurfactants (e.g., amphoacetate, CAPB) be used. It can be seen that amphoacetate maintains a wider isotropic region than CAPB (Tables 1 & 2 versus Table 3). Similarly CAPHS and coco betaine maintain a wider isotropic region than CAPB (Tables 4 and 5 versus 3). This is important in particular for fully formulated isotropic compositions.

When a mixture of C₁₀ and C_(coco) is used (see e.g. Table 2), which can be preferred in this invention, compared to mixture of C₁₀ and C₁₂ (Table 1) an isotropic region is achieved using lower amounts of C₁₀ glutamate. That is, less C₁₀ is needed to achieve soluble region (which also helps with lather production). Systems with glutamate plus amphoteric co-surfactant are hence preferred (e.g., amphoacetate or cocoamidopropylbetaine). Non-ionic surfactant is a preferred additional co-surfactant in a glutamate/co-surfactant system.

Our examples show that changing the distribution of the chain length on the glutamate surfactant can also provide preferred isotropic compositions. Thus, as use of glutamate is enhanced and the amount of cosurfactant minimized, the amount of lower chain length (e.g., C₈, C₁₀) glutamate can be lessened while still obtaining clear isotropic compositions at low pH. Using more of the higher chain length glutamate (e.g., C₁₂ to C₂₀) also helps maintain good foam values.

As indicated above, while C₁₀ should be minimized, depending on specific surfactant systems, in some embodiments of the invention ratio of C₁₀ to C₁₂ should be at least 1/5, possibly 1/3 and higher (although preferably no higher than 1/1) to ensure formation of isotropic compositions as defined.

Preferred stable, isotropic compositions are those with a ratio of C₁₀/C₁₂ acyl glutamate of about 1/3 and higher and with a ratio of lauroamphoacetate/acyl glutamate of about 1/1.7 and higher (up to 1/1). To ensure good foam performance and minimize costs, the ratio of C₁₀/C₁₂ acyl glutamate is preferably 1/1 and lower (preferably above 1/3) and the ratio of lauroamphoacetate/acyl glutamate should be 1/1 or lower.

There is thus the desired benefit achieved of preferred compositions with enhanced glutamate (using less cosurfactant) and greater amounts of higher chain glutamate (better foaming, especially good since there is less co-surfactant). Again, enhanced foam benefit from compositions based on isotropic surfactant chassis is seen whether final formulations are isotropic or anisotropic.

Preferably, the glutamates should be used in a concentration of ≥50% of surfactant system, more preferably ≥60%, more preferably >70%.

One composition which can be used comprises ≥50% glutamate and alkali metal alkyl (C₈-C₁₄) amphoacetate, preferably lauroamphoacetate. The composition may comprise a mixture of C₁₀ and C₁₂ or C₁₀ and C_(coco) glutamate (C_(coco) glutamate is glutamate with cocoyl chain length distribution as defined above). Mixtures of C₁₀ and C_(coco) are preferred if it is desired to minimize C₁₀ content since higher chain lengths typically provide better foaming. Such a mixture of C₁₀ and C_(coco) preferably has a C₈-C₁₀ chain length distribution wherein C₈-C₁₀ is present in an amount of more than 13%, preferably more than 15% of all R groups on glutamate salt as defined above.

In addition to absolute amounts of co-surfactant (it is preferred to minimize amount of co-surfactant), in some specific compositions we can define approximate minimum ratios of co-surfactant to glutamate needed to ensure isotropic formation. Thus, in amphoacetate/glutamate systems, the ratio of amphoacetate to glutamate is preferably about 1/7 and higher (up to 1/1) to maximize isotropic region. This may depend on chain lengths of glutamate and another preferred system is where mix of decanoyl and lauroyl glutamate is used and ratio of amphoacetate to glutamate is 1 to 1.7 and higher (preferably glutamate is primary surfactant overall).

Preferred stable, isotropic compositions are those with a ratio of C₁₀/C_(coco) acyl glutamate of about 1/3 and higher and with a ratio of lauroamphoacetate/acyl glutamate of about 1/7 and higher. To ensure good foam performance, minimize costs, and observe an enhanced viscosity, the ratio of C₁₀/C_(coco) acyl glutamate is preferably 1/1 and lower (preferably about 1/3 and above) and the ratio of lauroamphoacetate/acyl glutamate should be 1/1.7 or lower.

Another composition that may be used (although not preferred) comprises 50% glutamate and betaine, for example, cocoamidopropyl betaine. In such systems, glutamate comprises ≥60% of the surfactant system, more preferably ≥75%, more preferably ≥80%.

In a preferred system of the invention the ratio of amphoacetate to glutamate can be 1/19 and higher (preferably glutamate is primary surfactant). In such system, less co-surfactant is required to optimize isotropic region (e.g., compared to use of coamidopropylbetaine).

Similarly, another preferred embodiment comprises a surfactant system which is a mix of CAPHS and glutamate and where ratio of CAPHS to glutamate salts is as low as 1/19 and higher (up to 1/1). Again it is seen that less co-surfactant is needed to optimize isotropic region compared to CAPB.

Generally, preferred compositions are those in which salt of glutamate is selected from the group consisting of C10, C12 and C_(coco) glutamate and mixtures thereof. In a mixture comprising C_(coco), mixture preferably has a C₈-C₁₀ chain length distribution wherein C₈-C₁₀ is present in an amount of more than 13%, based on all R chain lengths on the glutamate salts. In such general composition, preferably amphoacetate is co-surfactant and preferably the ratio of amphoacetate to glutamate is 1/7 and higher, preferably 1/7 to 1/1. Another preferred co-surfactant is one selected from the group consisting of betaine, sultaine and mixtures thereof wherein the ratio of co-surfactant to glutamate is 1/19 and higher, preferably 1/19 to 1/1

Preferred stable, isotropic compositions are those with a ratio of C₁₀/C_(coco) acyl glutamate (using CAPHS, less co-surfactant is needed to obtain isotropic region compared to certain other co-surfactants, e.g., CAPB or amphoacetate) of about 1/7 and higher and with a ratio of CAPHS/acyl glutamate of about 1/19 and higher. To ensure good foam performance, minimize costs, and observe an enhanced viscosity, the ratio of C₁₀/C_(coco) acyl glutamate is preferably 1/1 and lower and the ratio of CAPHS/acyl glutamate is preferably 1/1 or lower.

When certain co-surfactants are used (e.g., CAPB), in addition to structurants of the invention, use of minimum amounts of fatty acid or salts may be required. Thus, for example, when CAPB is used, compositions require 0.1 to 2% by wt., preferably 0.1 to 1.5% by wt. fatty acids. Preferred fatty acids are C₈ to C₁₄, preferably lauric acid or myristic acid. Alternatively, if CAPB is used, use of 0.8 to 3.0% by wt., preferably 1.0 to 2.0% by wt. magnesium chloride is required.

Skin or Hair Benefit Agents

In the same composition of the invention, 0 to 30% by wt., preferably 0.1 to 10%, more preferably 0.1 to 5% by wt. skin or hair benefit agent is used. As the skilled person will understand, in the present composition, the benefit agent is a different compound than the surfactants indicated under the surfactant system. Hence, preferably, the benefit agent preferably is not a surfactant. Preferably the benefit agent is an oil soluble emollient or moisturizing oil. These are molecules which increase hydration by various mechanisms which may include prevention of water loss (occlusive agents), attracting moisture (humectants); or which restore natural moisturizing factors to the skin (e.g., amino-lipids). Preferred moisturizers include petrolatum and silicone. Preferably, moisturizer is a vegetable or triglyceride oil. Preferred oils include sunflower seed oil and soybean oil. The moisturizer may be an ester of long chain (C₁₄-C₃₀) fatty acid, such as isopropyl palmitate.

Some naturally restorative agents and moisturizers include:

-   -   a) vitamins such as vitamin A and E, and vitamin alkyl esters         such as vitamin C alkyl esters;     -   b) lipids such as cholesterol, cholesterol esters, lanolin,         sucrose esters, and pseudo-ceramides;     -   c) liposome forming materials such as phospholipids, and         suitable amphophilic molecules having two long hydrocarbon         chains;     -   d) essential fatty acids, poly unsaturated fatty acids, and         sources of these materials;     -   e) triglycerides of unsaturated fatty acids such as sunflower         oil, primrose oil, avocado oil, almond oil;     -   f) vegetable butters formed from mixtures of saturated and         unsaturated fatty acids such as Shea butter;     -   g) minerals such as sources of zinc, magnesium and iron; and     -   h) silicone oils, gums, modifications thereof such as linear and         cyclic polydimethylsiloxanes, amino, alkyl and alkyl aryl         silicone oil.

Water soluble benefit agents may also be used. Preferred water soluble agents include glycerin, sorbitol, polyalkylene glycol and mixtures thereof.

If used, depending on amount and miscibility of benefit agent in the isotropic surfactant chassis, the chassis may still maintain clarity. However, even if benefit agent renders chassis anisotropic, the low pH and foaming benefits discussed above are still retained.

Although compositions of the invention do not require external structurants, when oil soluble benefits as noted above are used, it is preferably to use structurants. Water soluble benefit agents (e.g., polyols) may also be used.

Structurant

Compositions of the invention comprise 0.1 to 10% by wt., preferably 0.5 to 7% by wt. of a structurant. The structurant may be a water soluble or water dispersible polymer which can be a cationic, anionic, amphoteric or nonionic polymer for enhancing viscosity.

Examples of water soluble/or dispersible polymers useful in the present invention include the carbohydrate gums such as cellulose gum, microcrystalline cellulose, cellulose gel, hydroxyethyl cellulose, hydroxypropyl cellulose, sodium carboxymethylcellulose, hydroxymethyl or carboxymethyl cellulose, methyl cellulose, ethyl cellulose, guar gum, gum karaya, gum traganth, gum Arabic, gum acavia, gum agar, xanthan gum and mixture thereof; modified and non-modified starch granules with gelatinization temperature between 30 to 85° C., and pregelatinized cold water soluble starch; polyacrylate; Carbopols; alkaline soluble emulsion polymer such as Aculyn 28, Aculyn 22 or Carbopol Aqua SF1; cationic polymers such as modified polysaccharides including cationic guar available from Rhone Poulenc under the trade name Jaguar C13S, Jaguar C14S, Jaguar C17, or Jaguar C16, BF Guar C17 from Lamberti, Aqua D4091 or Aqua D4051 from Aqualon; cationic modified cellulose such as UCARE Polymer JR30 or JR 40 from Amerchol; N-Hance 3000, N-Hance 3196, N-Hance CPX215 or N-Hance GPX 196 from Hercules; synthetic cationic polymer such as Merquat 100, Merquat 280, Merquat 281 and Merquat 550 by Nalco; cationic starches, e.g., StaLok® 100, 200, 300 and 400 made by Staley Inc.; cationic galactamannans based on guar gum of Galactasol 800 series by Henkel, Inc.; Quadrisect Um-200, and Polyquaternium-24.

Gel forming polymers such as modified or non-modified starch granules, xanthan gum, Carbopol, alkaline-soluble emulsion polymers and cationic guar gum such as Lamberti BF Guar C17, and cationic modified cellulose such as UCARE Polymer JR 30® or JR 40® are particularly preferred for this invention.

A preferred structuring copolymer is the polymerization product (e.g., additive polymerization product) of (1) a first ethylenically unsaturated monomer; (2) a second ethylenically unsaturated monomer; (3) (meth)acrylate monomer and (4) associative monomer (generally random in structure; preferably copolymers are linear).

The first monomer of (1) may be di-acid of formula: HOOC—CR¹═CR²—COOH  (I),

-   -   a cyclic anhydride precursor of diacid (I), the anhydride having         the formula:

-   -   and combinations thereof,         wherein R¹ and R² are individually selected from H, C₁-C₃ alkyl,         phenyl, chlorine and bromine and, in one or more embodiments,         are preferably individually selected from H and C₁-C₃ alkyl.

Preferred monomers include maleic acid and maleic acid anhydride. It may comprise 0 to 10%, preferably 0.1 to 5% by wt. on total wt. of monomer charge.

The second monomer (2) can be acrylic acid, methacrylic acid and combinations thereof. It can be used at 15-60% by wt. based on total monomer charges.

The (meth)acrylate (3) monomer can be C₁ to C₈ alkyl esters of acrylic acid, C₁ to C₈ alkyl esters of methacrylic acid and combinations and can be 30-75% by wt. based on total monomer charge.

The associative monomer (4) has the formula: R⁴—CH═C(R³)—C(O)—O—(R⁵O)_(a)—R⁶  (III)

-   -   wherein:         -   R³ and R⁴ are independently selected from H and C₁₋₃ alkyl,         -   each R⁵O is independently an oxyalkylene unit having from 2             to 4, preferably from 2 to 3 carbon atoms,         -   R⁶ is selected from:             -   linear and branched alkyl having from 8 to 40,                 preferably from 8 to 30, more preferably from 10 to 22                 carbon atoms, and             -   alkaryl, the alkyl group of which has from 8 to 40,                 preferably from 8 to 30, more preferably from 10 to 22                 carbon atoms, such alkyl group being linear or branched,                 said alkaryl preferably being alkylphenyl; and         -   a has a value of from 6 to 40, preferably from 15 to 35,             most preferably from 20 to 30.

Of particular interest in one or more embodiments is an associative monomer of the formula: CH₃[CH₂]_(b)—CH₂—[OCH₂CH₂]_(a)—O—C(O)C(R³)═CH(R⁴)  (IV) in which R³, R⁴ and a are as described above, and b has a value of from 6 to 38, preferably from 6 to 28, and more preferably from 8 to 20.

In the Formula III and Formula IV monomers, R³ is preferably a methyl group and R⁴ is preferably H. In the above described associative monomers, a and b represent the number of their respective oxyalkylene and —CH₂— repeat units and generally are integers. In one or more embodiments of interest a is greater than or equal to b.

The associative monomer may be employed in amounts of from 1 to about 25 wt. %, preferably from 2 to 20 wt. %, and more preferably from 2 to 15 wt. %, based on total monomer added. In one or more embodiments of particular interest the amount of associative monomer employed is from 5 to 12 wt. %, based on total monomer added.

In some compositions a structurant which has been found particularly effective to maintain clarity and stability is copolymer of the following formula:

-   -   wherein a, b, c, d and e represent the percentage by weight that         each repeating unit monomer is contained within the copolymer;     -   A is a polyacidic vinyl monomer selected from the group         consisting of maleic, fumaric, itaconic, citraconic and acid         combinations thereof and anhydrides and salts thereof; and     -   B is acrylic or methacrylic acid or a salt thereof;     -   C is a C₁-C₈ ester of acrylic acid or methacrylic acid;     -   D is an associative monomer of formula

-   -   wherein each R₂ is independently H, methyl, —C(═O)OH, or         —C(═O)OR₃;     -   R₃ is a C₁-C₃₀ alkyl;     -   T is —CH₂C(═O)O—, —C(═O)O—, —O—, —CH₂O—, —NHC(═O)NH—, —C(═O)NH—,         Ar—(CE₂)_(z)-NHC(═O)O—, —Ar—(CE₂)_(z)-NHC(═O)NH—, or         —CH₂CH₂NHC(═O)—;     -   Ar is divalent aryl;     -   E is H or methyl;     -   z is 0 or 1;     -   k is an integer in the range of 0 to 30; and m is 0 or 1;     -   with the proviso that when k is 0, m is 0, and when k is in the         range of 1 to 30; m is 1;     -   (R₄O)_(n) is polyoxyalkylene, which is a homopolymer, a random         copolymer, or a block copolymer of C₂-C₄-oxyalkylene units,         wherein R₄ is C₂H₄, C₃H₆, C₄H₈, or a mixture thereof, and n is         an integer in the range of 5 to 250;     -   Y is —R₄O—, —R₄H—, —C(═O)—, —C(═O)NH—, R₄NHC(═O)NH—, or         —C(═O)NHC(═O)—; and     -   R₅ is substituted or unsubstituted alkyl selected from the group         consisting of C₈-C₄₀ linear alkyl, C₈-C₄₀ branched alkyl, C₈-C₄₀         carbocyclic alkyl, C₂-C₄₀ alkyl-substituted, phenyl,         aryl-substituted C₂-C₄₀ alkyl, and C₈-C₈₀ complex ester; wherein         the R₅ alkyl group optionally comprises one or more substituents         selected from the group consisting of hydroxy, alkoxy, and         halogen; and     -   E when present is a cross linking monomer for introducing         branching and controlling molecular weight, the cross linking         monomer comprising polyfunctional units carrying multiple         reactive functionalization groups selected from the group         consisting of vinyl, allylic and functional mixtures thereof,         the groups A, B, C, D and E being covalently bonded one to         another in a manner selected from a random, a block or a         cross-linked copolymer format.

Amounts of “a” may range from about 0 to 10%, preferably 0.1 to about 5% by weight; amounts of “b” may range from about 10 to about 80%, preferably 15 to 60% by weight; amounts of “c” may range from about 30 to about 85%, preferably 30 to 75% by weight; amounts of “d” may range from about 1 to about 25% by weight; and amounts of “e” may range from 0 to about 5% by weight of the total copolymer.

Some compositions may contain water-soluble polymers in amounts of 0.005 to 5% by wt.

Examples of water soluble polymers include high molecular weight polyethylene glycols such as Polyox® WSR-205 (PEG 14M), Polyox® WSR-N-60K (PEG 45M), and Polyox® WSR-301 (PEG 90M); the carbohydrate gums such as cellulose gum. hydroxyethyl cellulose, hydroxypropyl cellulose, sodium carboxymethylcellulose, methyl cellulose, ethyl cellulose, guar gum, gum karaya, gum tragacanth, gum arabic, gum acacia, gum agar, and xanthan gum; modified starch granules and pregelatinized cold water soluble starch; cationic polymer such as modified polysaccharides including cationic guar available from Rhodia under the trade name Jaguar®; cationic modified cellulose such as UCARE Polymer JR 30 or JR 40 from Amerchol; N-Hance® 3000, N-Hance® 3196, N-Hance® GPX 215 or N-Hance® GPX 196 from Hercules; synthetic cationic polymers such as Merquat® 100, Merquat® 280, Merquat® 281 and Merquat® 550 sold by Nalco. The water soluble polymers may be used individually or as combinations of two or more polymers from the same or different classes. High molecular weight polyethylene glycols Polyox® WSR-301 (PEG 90M) and Polyox® WSR-N-60K (PEG 45M) and guar derivatives such as Jaguar® S, Jaguar® C17, and Jaguar® C13, and synthetic cationic polymers such as Merquat® 100 are particularly desired.

Preservatives

Personal product formulations provide good media for growth of microbes. Microbial action can be manifested in terms of hydrolysis, oxidation or reduction and may cause off-odors, changes in color, adverse change in pH, breaking of emulsions, and changes in product texture. Thus good preservation systems are required to prevent microbial growth, spoiling of product, and infection of skin and hair. The preservative should be effective against Gram-negative and Gram-positive bacteria as well as fungi (molds and yeasts).

An effective preservative is a chemical agent which will prevent microbial growth in the product, making it safe and increasing shelf life.

Optimal preservation system should provide broad spectrum activity and be effective over the shelf-life of the product. As microorganisms multiply in the aqueous phase of formulations, it should also be water-soluble. Where formulations contain appreciable levels of oils, the system should favor partitioning into the aqueous phase. Ideally, the preservation system should be effective over wide pH range, colorless and safe in use. It should be non-irritating, non-sensitizing and preferably non-poisonous. Ideally, while eliminating pathogenic organisms in the formulation while in storage, it should leave symbiotic organisms on the skin in peace after application of the formulation to the skin, hair or mucous membrane.

Some preferred preservatives include:

-   -   1) Parabens, for example, methyl-, ethyl-, propyl-, iso-butyl-,         and butyl-paraben;     -   2) Formaldehyde-releasing preservatives, for example,         formaldehyde, quaternium-15, dimethyl-dimethyl (DMDM) hydantoin,         imidazolidinyl urea, diazolidinyl urea, sodium         hydroxymethylglycinate, and 2-bromo-2-nitropropane-1,3-diol;     -   3) Isothiazolones, such as chloromethyl-isothiozolinone (CMIT),         methyl-isothiazolinone (MIT) or benz-isothiazolinone (BIT);     -   4) Halogen-organic actives, such as idopropynyl butylcarbamate         and methyl-dibromo glutaranitrile;     -   5) Organic acids such as benzoic acid, dehydroacetic acid,         salicylic acid, lactic acid and sorbic acids;     -   6) Other, including chloroacetamide, phenyloxyethanol and         triclosan.

Additional suitable preservatives for personal care products can be found in “Preservatives for Cosmetics Manual, 2^(nd) edition”, by David S. Steinbens, 2006 and in “Preservatives for Cosmetics”, D. C. Steinberg, Allured Publishing Corp., ISBN #0-93170-54-5. Such agents are typically employed at 0.1-1%, more preferably at 0.5-0.7% of the personal product formulation. The organic acids noted are particularly preferred. Especially preferred are organic acids having pKa between about 4.0 and 5.5, preferably 4.0 and 5.0.

No preservative is ideal for all situations. For example, parabens are relatively non-irritant, but partition in favor of oil phase and are inactivated by some surfactants. Formaldehyde-retaining preservative have broad effectiveness spectrum, but are irritant and banned in some countries.

Applicants have filed a co-pending application directed to low pH based isotropic compositions having specific preservative systems.

Compositions of that application, and certainly compositions of this invention having preferred pH of about 3.0 to 5.1, preferably will comprise the organic acids noted above as preservative. Specifically, organic acids having pKa of 4.0 to 5.5, preferably 4.2 and 5.1 are preferred.

More specifically compositions preferably have pH which is less than one pH unit, more preferred less than 0.5 pH unit, above the pKa of the organic acid. Within such tight pH range, the organic acid will stay largely in undissociated form which is the form required for activity against microorganisms.

Thus, for example, since pKa of benzoic acid is 4.2, it is ideally suited to be used in composition of pH less than 5.2 (as in preferred embodiments of the invention), preferably at or less than 4.7.

As indicated, benzoic acid is a preferred preservative.

Optionally, the compositions of this invention may further comprise one or more additional ingredients. Non-limiting examples of such additional ingredients are, for example, colorants, pigments, opacifiers, fragrance (whether encapsulated or present as free-fragrance), emotive oils, vitamins and vitamin derivatives, abrasives, optical agents (including for example, reflective particles and interference pigments), pH adjusters, plant extracts, essential oils, preservatives, antioxidants, antimicrobials, viscosity modifiers, humectants, beard wetting agents, sensory agents, fatty acid soap, and skin and/or hair benefit agents (e.g., aloe, allantoin, panthenol, alpha-hydroxy acids, phospholipids, botanical oils, and amino acids to name a few). The selection and amount of any individual additional ingredient depends upon factors that include the particular ingredient, the properties desired, and the intended use of the composition in which it is employed. For example, fragrance is typically employed in an amount of 0.1 to 3.0% by weight of the composition, or higher. For many compositions, the total amount of such additional ingredients is 0.01 to 30% by weight, more particularly, 0.1 to 15% by weight, even more particularly, 1 to 10% by weight, based on the total weight of the composition. In one or more embodiments, the total amount of such additional optional ingredients is 0.5 to 5% by weight. Other ingredients, for example fatty acid soap, may be present at levels up to 10% by weight, based on the total weight of the composition.

Compositions are aqueous based and comprise typically 30-90% by wt. water. Water is balance after all ingredients noted above are accounted for.

Protocols

Clarity

Transparency (clarity) of a sample is measured by measuring the optical absorbance at wavelength of λ=550 nm. The fully formulated samples (about 300 μl) are added into a 96-well plate without dilution and read by a microplate Reader (SpectraMax® 340PC, Molecular Device). An ideally transparent sample has zero absorbance (i.e., 100% transmission). In this invention, a sample with absorbance of below 1.5, more preferably below 1, more preferably below 0.5, even more preferably, below 0.2 is defined as giving visually acceptable transparency (clarity).

Structure (as Defined by Initial Bulk Viscosity)

The structures of liquid cleansing formulations are characterized by initial bulk viscosity of compositions when freshly prepared. The viscosity of composition is measured by a stress controlled rheometer (AR-G2, TA Instruments) at 25° C. A sample with good structure should have bulk viscosity (at shear rate of 1.0 s⁻¹)>1,000 cps, preferably more than 5,000 cps, more preferably >10,000 cps. A preferred upper range is about 50,000 cps.

Phase Stability (as Defined by Viscosity Maintenance and No Phase Separation)

The term phase stability refers to several points. First, the compositions remain optically clear and maintain bulk viscosity. Specifically, after a storage period at 4° C., 25° or 50°, there is no significant change (<±30%) from when measured before and when measured after two weeks. Secondly, the compositions maintain phase homogeneity and integrity without noticeable phase separation after storage at 4° C., 25° or 50° for the period of two weeks.

It should be understood that the two week storage period is at one of the selected temperature conditions, and is not variable over the storage time.

Preparation of Formulations

The liquid formulations were prepared at room temperature or elevated temperature (e.g. 70° C.) to completely dissolve all ingredients into water in order to form a homogeneous phase.

Structuring ingredients such as acrylate copolymer, starch or xanthan gum, etc. were dispersed into water by an overhead mixer to fully activate their structuring capability. For compositions with solid ingredients (e.g., fatty acids), mixing at a temperature 5-10 degree Celsius higher than the melting point is needed. All the ingredients were mixed continuously until uniform after pH adjustment by citric acid.

EXAMPLES Example 1

Stability Map of the lauroyl glutamate/amphoacetate system for 15% total surfactant and pH 4.5. Lauroyl glutamate was mixed with decanoyl glutamate as indicated. Symbol I=isotropic system with absorbance value at 550 nm below 0.2, X=two-phase system. In these systems, the left column represents % of C₁₀ relative to % of C₁₀ and C₁₂ so that, for example, 75 represents a system in which 75% of the total glutamate present is C₁₀ and 25% is C₁₂. The top row is % of amphoacetate with the balance being glutamate. Thus, 12.5 represents a system in which 87.5% of the surfactant is glutamate blend and 12.5% is amphoacetate. The total surfactant present is 15% in all cases, with the remainder being water with a minor amount of citric acid.

TABLE 1 % decanoyl glutamate % Na lauroamphoacetate [C₁₀/(C₁₀ + C₁₂)] × 100 0 12.5 25 37.5 50 100 I I I I I 75 I I I I I 50 X X X I I 25 X X X I I 0 X X X X X

It will be seen that, for this example, preferred stable, isotropic compositions are those with a ratio of C₁₀/C₁₂ acyl glutamate of about 1/3 and higher and with a ratio of lauroamphoacetate/acyl glutamate of about 1/1.7 and higher. To ensure good foam performance and minimize costs, the ratio of C₁₀/C₁₂ acyl glutamate should be 1/1 and lower, preferably above 1/3, and the ratio of lauroamphoacetate/acyl glutamate should be 1/1 or lower.

Example 2

Stability Map of the cocoyl glutamate/amphoacetate system for 15% total surfactant and pH 4.5. Cocoyl glutamate was mixed with decanoyl glutamate as indicated. Symbol I=isotropic system with absorbance value at 550 nm below 0.2, X=two-phase system. Percentages are measured as noted in Table 1 of Example 1.

TABLE 2 % decanoyl glutamate % Na lauroamphoacetate [C₁₀/(C₁₀ + C_(coco))] × 100 0 12.5 25 37.5 50 50 I I I I X 37.5 I I I I X 25 X I I I X 0 X X I I I

It will be seen that preferred stable, isotropic compositions are those with a ratio of C₁₀/C_(coco) acyl glutamate of about 1/3 and higher and with a ratio of lauroamphoacetate/acyl glutamate of about 1/7 and higher. To ensure good foam performance, minimize costs, and observe an enhanced viscosity, the ratio of C₁₀/C_(coco) acyl glutamate should be 1/1 and lower (preferably about 1/3 and above) and the ratio of lauroamphoacetate/acyl glutamate should be 1/1.7 or lower.

Example 3

Stability Map of the cocoyl glutamate/CAPB system for 15% total surfactant and pH 4.5. Cocoyl glutamate was mixed with decanoyl glutamate as indicated. Symbol I=isotropic system with absorbance value at 550 nm below 0.2, X=two phase system. Percentages are measured as noted in Table 1.

TABLE 3 % decanoyl glutamate % CAPB [C₁₀/(C₁₀ + C_(coco))] × 100 0 12.5 25 37.5 50 50 I I X X X 37.5 I X X X X 25 X X X X X 0 X X X X X

As seen from Examples 1-3, when we use a mixture of C₁₀ and C_(coco) (Table 2) compared to mixture of C₁₀ and C₁₂ (Table 1), an isotropic region is achieved using much lower amounts of C₁₀ glutamate. That is, less C₁₀ is needed to achieve soluble region (which also helps with lather production). Systems are glutamate plus co-surfactant (e.g., amphoacetate or cocoamidopropylbetaine). When co-surfactant used is CAPB rather than amphoacetate (Table 3 versus Table 2), some solubility benefit at lesser level of C₁₀ is lost. Even where solubility is lost, however, benefits of low pH (for alternative preservation systems) and foam from using high glutamate surfactant chassis are retained.

Example 4

Stability Map of the cocoyl glutamate/cocoamidopropyl hydroxyl sultaine (CAPHS) system for 15% total surfactant and pH 4.5. Cocoyl glutamate was mixed with decanoyl glutamate as indicated. Symbol I=isotropic system with absorbance value at 550 nm below 0.2, X=two phase system. Percentages are measured as noted in Table 1.

TABLE 4 % decanoyl glutamate % CAPHS [C₁₀/(C₁₀ + C_(coco))] × 100 0 5 12.5 25 37.5 50 50 I I I I I I 37.5 I I I I I I 25 X I I I I I 0 X X X X I I

It will be seen that preferred stable, isotropic compositions are those with a ratio of C₁₀/C_(coco) acyl glutamate (using CAPHS, less co-surfactant is needed to obtain isotropic region compared to certain other co-surfactants, e.g. CAPB or amphoacetate) of about 1/7 and higher and with a ratio of CAPHS/acyl glutamate of about 1/19 and higher. To ensure good foam performance, minimize costs, and observe an enhanced viscosity, the ratio of C₁₀/C_(coco) acyl glutamate should be 1/1 and lower and the ratio of CAPHS/acyl glutamate should be 1/1 or lower.

Example 5

Stability Map of the cocoyl glutamate/coco betaine system for 15% total surfactant and pH 4.5. Cocoyl glutamate was mixed with decanoyl glutamate as indicated. Symbol I—isotropic system with absorbance value at 550 nm below 0.2, X=two phase system. Percentages are measured as noted in Table 1.

TABLE 5 % decanoyl glutamate % cocoyl betaine [C₁₀/(C₁₀ + C_(coco))] × 100 0 5 12.5 25 37.5 50 50 I I I I I I 37.5 I I I I I I 25 X I I I I I 0 X X I I I I

It will be seen that preferred stable, isotropic compositions are those with a ratio of C₁₀/C_(coco) acyl glutamate of about 1/7 and higher and with a ratio of coco betaine/acyl glutamate of about 1/19 and higher (less co-surfactant needed to obtain isotropic regions compared to use of certain other co-surfactants). To ensure good foam performance, minimize costs, and observe an enhanced viscosity, the ratio of C₁₀/C_(coco) acyl glutamate should be 1/1 and lower and the ratio of coco betaine/acyl glutamate should be 1/1 or lower.

As seen from Examples 2, 4 and 5, when we use a mixture of C₁₀ and C_(coco) glutamates along with a co-surfactant chosen from the preferred list of amphoteric surfactants, a broad, isotropic, stable region results. More specifically, blending shorter chain length glutamates (decanoyl glutamate) with longer chain length glutamates (cocoyl glutamate) yields isotropic systems at pH 4.5 in which glutamate comprises 100% of the surfactant system. Further, addition of preferred amphoteric co-surfactants to glutamate blends results in isotropic systems in which glutamate comprise ≥50% of the surfactant system and 100% of the total anionic surfactant while allowing for a glutamate blend richer in longer chain lengths, which enhances foaming. Again, even where benefit agents in final system may form anisotropic compositions, foam benefits are retained.

Examples 6-8

For Examples 6-8, finished formulations were prepared by adding the surfactants, starch, and 70% of the free water into a tared vessel immersed in a water bath and with overhead mixing. The components are stirred until uniformly mixed and then the stirring continued as the water bath temperature is raised to 70° C. Once at temperature, the Jaguar (predispersed in glycerin) and PEG are added along with the citric acid. Cooling is initiated and the other components added once the water bath reaches 35° C. The final pH and water content are then adjusted.

Example 6 Example 7 Example 8 % % % % on 100% on 100% on 100% Chemical/ active as active active active Trade Name supplied basis basis basis Water 100 84.27 83.85 79.35 Puregel B990 100 0.00 0.00 4.5 (modified starch; thickener) Lauroyl 100 6.60 6.60 0.00 Glutamate Cocoyl Glutamate 100 0.00 0.00 6.60 Na Lauroyl 30 0.00 0.00 0.00 Sarcosinate Sodium 29 5.49 5.49 5.49 Lauroamphoacetate Jaguar C-14 100 0.3 0.3 0.3 Glycerin 100 2.00 2.00 2.00 PEG 45M 100 0.05 0.05 0.05 Citric acid 50 1.25 1.25 1.25 Sodium benzoate 100 0.00 0.5 0.5 (preservative) Butylated 100 0.00 0.00 0.00 Hydroxytoluene (BHT) Methylisothiazolinone 9.5 0.01 0.00 0.00 (MIT) (preservative) Glydant Plus Liquid 20 0.07 0.00 0.00 (preservative) EDTA 39 0.05 0.05 0.05 (ethylenediamine Tetraacetic acid) (sequestrant) Total 100 100 100 pH 4.5 4.5 4.5

Example 6 is typical of a conventional preservation system, which can be used over a wide pH range but whose application is regionally restricted. In contrast, Example 7 illustrates a preservation system which is preferred in those regions but which will only function at pH 5.0 and below. The example formulation provides an effective product form in which to practice this preservation system. Both examples yielded stable, isotropic, single phase systems. Example 8 is an example of a finished formulation which contains optional benefiting ingredients (Puregel® B990 in this case, a starch thickening agent) which render the final system anisotropic, though still stable against physical phase separation.

Examples 9-11

For Examples 9-11, finished formulations were prepared as described for Examples 6-8.

Example 9 Example 10 Example % % % 11 % active on 100% on 100% on 100% Chemical/ as active active active Trade Name supplied basis basis basis Water 100 77.99 74.75 64.44 (modified polyacrylate; 34 0.5 0.5 0.0 thickener)¹ Puragel B990 (modified 100 0.0 0.0 4.50 starch thickener) Carbopol 980 100 0.0 0.0 0.6 Decanoyl 100 4.39 4.39 0.0 Glutamate Cocoyl Glutamate 23 4.39 4.39 6.6 Na Lauroyl Sarcosinate 30 0.95 0.95 0.0 Cocamidopropyl hydroxy 40 5.28 6.00 0.0 sultaine Sodium 28 0.0 0.0 5.40 lauroamphoacetate Jaguar C-14 100 0.0 0.1 0.30 Glycerin 100 5.00 2.00 6.0 PEG-14M 100 0.0 0.0 0.5 PEG-45M 100 0.05 0.05 0.0 Soybean Oil 100 0.0 3.0 0.0 Hydrogenated Soybean 100 0.0 2.0 0.0 Oil Petrolatum 100 0.0 0.0 8.75 Polybutene (H-300) 100 0.0 0.0 0.5 Citric acid 50 1.32 1.32 1.15 Sodium benzoate 100 0.00 0.5 0.0 (preservative) butylated hydroxytoluene 100 0.00 0.00 0.10 (BHT) Methylisothiazolinone 9.5 0.01 0.00 0.01 (MIT) (preservative) Glydant Plus Liquid 20 0.07 0.00 0.0 (preservative) EDTA (ethylenediamine 39 0.05 0.05 0.05 tetraacetic acid) (sequestrant) Fragrance 100 0.0 0.0 1.10 Total 100 100 100 pH 4.8 4.8 4.8 ¹This is a copolymer which is the polymerization product of (by weight of total polymer) (a) about 40 to 70% ethyl acrylate; (b) 20 to 50% methacrylic acid; (c) 0.1 to 3% maleic anhydride and; (d) 2 to 15% of an associative monomer (for example, Component D of Formula V defined above).

Example 9 is typical of a conventional preservation system, which can be used over a wide pH range but whose application is regionally restricted. In contrast, Example 10 illustrates a preservation system which is preferred in those regions but which will only function at pH 5.0 and below. The example formulation provides an effective product form in which to practice the preservation system. Both examples yielded stable, isotropic, single phase surfactant chassis. Example 10 is an example of a finished formulation which contains optional benefiting ingredients (soybean oil and hydrogenated soybean oil in this case, an emollient oil) which render the final system anisotropic, though still stable against physical phase separation. Similarly, Example 11 is an example of a finished formulation which contains optional benefiting ingredients (petrolatum and polybutene, an emollient oil and sensory modifier, respectively) which render the final system anisotropic, though still stable against physical phase separation.

Example 12-14 Comparatives 15-20 12 13 14 15 16 17 18 19 20 Component Sodium Lauroyl Glutamate 9% 6%   9%   9% 9%   9% 6% 9%   9% Cocamidopropyl 3% 6%   3%   3% 3%   3% 6% 3%   3% Betaine Acrylates Copolymer 1.20% 2% 1.80%   1.80% (Carbopol ® Aqua SF1 polymer from Lubrizol) Structurant (structurant of 1.5%  1.5%   1.8%  1.8% 1.8%  examples 9-11; see Footnote 1) Starch (Pure-Gel ® B990)* 4.50% Lauric Acid 1% 0.30% 0.50% 0.50% Myristic Acid 0.30% 0.50% Cocomonoethanolamide 0.90%   0.90% 0.90% 0.90%   (CMEA) NaCl 1%   1% 0.50% 1% 0.50% 1% 2% 1.20% MgCl2 1.20%   0.50% 0.50%   Fragrance 1% 1% 0.75% 0.75% 0.75%   0.75% 1% 1%   1% Preservative 0.001%    0.001%    0.001%  0.001%  0.001%    0.001%  0.001%    0.001%    0.001%  Kathon Kathon Kathon Kathon Kathon Kathon Kathon Kathon Kathon pH 5.5 5.5 5.5 5.5 5.5 5.5 5.5 5.5 5.5 result good good good low low good low low low viscosity, viscosity, viscosity, viscosity viscosity viscosity viscosity viscosity viscosity stable stable stable and hazy and opaque but hazy and hazy and hazy and hazy and clear and clear and clear *Structurant of Examples 9-11 From Examples 12-14 versus Comparatives 15-20, several things are noted. With respect to comparative 17-20, the absence of claimed structurant of the invention fails to provide compositions which are both clear and well structured (well structured compositions must themselves meet 3 criteria: be phase stable, have initial viscosity greater than 1000 cps and maintain viscosity defined in protocol). In compositions 15-16, level of fatty acid in composition is not sufficiently high to prevent phase separation. Similarly, in compositions 15 and 16, there is not sufficient MgCl2 to help create clear, structured compositions. Compositions which are opaque or hazy fail to meet clarity protocol definitions *A modified dent corn starch from Grain Processing Corporation. Example 21-22 Comparatives 23-29 21 22 23 24 25 26 27 28 29 Component Sodium Lauroyl Glutamate   9% 9% 9%   9%   9%   9% 9% 9% 9% Cocamidopropyl   3% 3% 3%   3%   3%   3% 3% 3% 3% Betaine (CAPB) Structurant (same  1.5% 1% Structurant (for comparatives) structurant as Examples 9-11; see Footnote 1) Starch (Pure-Gel ® B990) 10%  Polyacrylate-1 crosspolymer 1.20% (Carbopol ® Aqua CC polymer from Lubrizol) Carbopol 980 0.50% Ammonium acryloyl 1.50% 1.80%   dimethyltaurate/carboxy ethyl acrylate crosspolymer* PEG6000-Distearate 1% Xanthan Gum 2% (In 6%    Glycerine) Lauric Acid 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 0.1-2.0 CMEA 0.90%   NaCl 0.25% 0.60%   1% 0.25% 0.25% 0.50% 0.20%   0.40%   0.50%   Need Fragrance 0.75% 0.75%   1% 0.75% 0.75% 0.75% 1% 0.75%   1% Fragrance Preservative Kathon Kathon 0.001%    0.001%  0.001%  0.001%  0.5%  0.5%  0.001%    0.001%  0.001%    Kathon Kathon Kathon Kathon Benzoate Benzoate Kathon pH 5.5 5.5 5.5 5.5 5.5 5 5 5 5 Result good good low low low low low hazy hazy viscos- viscos- viscos- viscos- viscos- viscos- viscos- ity, ity, ity ity ity ity ity stable stable and hazy and hazy and hazy and hazy and hazy and clear and clear In Examples 21-22 and comparative 23-29, compositions are still not both clear and well structured (as defined) unless structurants of the invention are used. When other structurants are used, compositions are thin (or stringy) and/or they are not clear. Compositions which are hazy fail to meet clarity protocol definitions. *Aristoflex ® TAC polymer from Clariant Example 30-31 Comparison 32-35 30 31 32 33 34 35 Component Sodium Cocoyl Glutamate   6%   6%   6%   6%   6%   6% (Amisoft CS11, Ajinomoto) Sodium Lauroamphoacetate   6%   6%   6%   6%   6%   6% Structurant (same as Examples 9-11; see  0.5%  0.5% Structurant Structurant Structurant Structurant Footnote 1) Starch (Pure-Gel ® B990)   4% Ethycellulose polymer with viscosity 0.50% ranging about 35-110 mPa · s (cP)* Aristoflex TAC (as in Examples 26-27) 2 PEG 90M** 0.05% 0.04% 0.03% 0.04% NaCl 0.40% 0.50% Sodium Benzoate 0.50% 0.50% 0.50% 0.50% 0.15% 0.50% Glycerine 0.50% 0.35% 0.30% 0.40% Fragrance 0.80% 0.80% 1.20% 0.80% 0.80% 0.80% pH 5 5 4.8 4.8 4.8 5 Result good good good low low good viscosity, viscosity, viscosity viscosity viscosity viscosity stable stable but opaque but hazy and clear and clear Examples 30-31 and comparatives 32-35 show that, when amphoacetate is used as co-surfactant, lower amounts of structurant may be used (while not wishing to be bound by theory, we believe this is because these surfactants help partially structure). However, structurants must still be those of the invention (see comparative Examples 32-35) to ensure both structure, stability and clarity. Compositions which are opaque or hazy fail to meet clarity protocol definitions. *Ethocel ® polymers 40-100 from Dow ®. **Ethylene glycol with average 90M ethylene glycol units. 

The invention claimed is:
 1. Cleansing composition comprising: a) 0.5 to 35% by wt. total composition of a surfactant system comprising anionic surfactant comprising salt of acyl glutamate, wherein salt of acyl glutamate is present at 50% or more of all surfactant present, and wherein the surfactant system further comprises 0 to 20% by wt. total composition of a co-surfactant, wherein co-surfactant are surfactants which are not anionic, selected from the group consisting of nonionic, cationic, amphoteric surfactants and mixtures thereof; b) 0% to 30% by wt. total composition water-soluble or oil-soluble skin or hair benefit agent not being a surfactant; c) 0.1 to 10% of a structuring polymer which is a polymerization product of: i) 0 to 10% by wt. of total monomer of a first ethylenically unsaturated monomer selected from the group consisting of: A) diacids of formula HOOC—CR¹═CR²—COOH (I); B) a cyclic anhydride precursor of diacid (I), having the formula:

C) and combination thereof, where R¹ and R² are individually selected from H, C₁-C₃ alkyl, phenyl, chlorine and bromine; ii) 15 to 60% by wt. total monomer of a second ethylenically unsaturated monomer selected from the group consisting of acrylic acid, methacrylic acid and mixtures thereof; iii) 30 to 75% by wt. of total monomer of a (meth)acrylate monomer which is selected from the group consisting of C₁ to C₈ esters of acrylic acid, C₁ to C₈ esters of methacrylic acid and mixtures thereof; and iv) 1 to 25% by wt. of total monomer of an associative monomer having the formula: R⁴—CH═C(R³)—C(O)—O—(R⁵O)_(a)—R⁶ wherein: R³ and R⁴ are independently selected from H and C₁₋₃ alkyl, each R⁵O is independently an oxyalkylene unit having from 2 to 4carbon atoms, R⁶ is selected from: linear and branched alkyl having from 8 to 40 carbon atoms, and alkaryl, the alkyl group of which has from 8 to 40 carbon atoms, such alkyl group being linear or branched; and a has a value of from 6 to 40; and d) water and wherein salt of glutamate comprises a mixture of C₁₀ and C_(coco) glutamate, wherein the mixture of C₁₀ and C_(coco) has a C₈-C₁₀ chain length distribution wherein C₈-C₁₀ is present in an amount of more than 13%, or salt of glutamate comprises a mixture of C₁₀ and C₁₂ glutamate, wherein the ratio of C₁₀ to C₁₂ is at least 1/5, wherein pH of composition is 5.5 or below.
 2. A composition according to claim 1, wherein the composition is clear isotropic, wherein clear isotropic is defined by absorbance value of 1.0 or below when measured at wavelength of 550 nm, adding 300 μl into a 96-well plate without dilution.
 3. A composition according to claim 1, wherein salt of glutamate comprises a mixture of C₁₀ and C_(coco) glutamate wherein the mixture of C₁₀ and C_(coco) has a C₈-C₁₀ chain length distribution wherein C₈-C₁₀ is present in an amount of more than 13%.
 4. A composition according to claim 1, further comprising 0.1% to 10% by wt. benefit agent not being a surfactant.
 5. A composition according to claim 1 wherein pH of composition is 4.0 to 6.0.
 6. A composition according to claim 1, wherein pH is 4 to 5.5.
 7. A composition according to claim 1, wherein co-surfactant is cocoamidopropylbetaine and which comprises 0.1 to 2% C₁₀-C₁₄ fatty acid.
 8. Composition according to claim 1, wherein co-surfactant is CAPB and level of MgCl₂ is 0.8% to 3.0%.
 9. A composition according to claim 1, which has initial bulk viscosity at shear rate of 1.0 s⁻¹ of greater than 1,000 cps.
 10. A composition according to claim 1, which remains clear and whose bulk viscosity at shear rate of 1.0 s⁻¹, measured by a stress-controlled rheometer, remains significantly stable (±30%) from when measured before and after two weeks at storage temperatures of 4° C., 25° C. and 50° C.; and which composition has no visible phase separation after storage of two weeks at temperatures of 4° C., 25° C. and 50° C.
 11. A composition according to claim 1, subparagraph (iv), wherein the alkaryl group is alkylphenyl. 